H-Glu-Tyr-OH
PubChem CID: 515717
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| Compound Synonyms | H-Glu-Tyr-OH, 3422-39-7, Glu-Tyr, L-Glutamyl-L-Tyrosine, glutamyltyrosine, EY dipeptide, glutamyl-tyrosine, alpha-Glu-Tyr, E-Y Dipeptide, MFCD00063199, alpha-L-Glu-L-Tyr, L-Glu-L-Tyr, L-Glutamyl-L-Tyrosin, Glutamate Tyrosine dipeptide, Glutamate-Tyrosine dipeptide, L-alpha-glutamyl-L-tyrosine, SCHEMBL159463, CHEBI:73513, DTXSID90326069, EY, HY-P4595, DA-53975, FG108041, L-Tyrosine, L-.alpha.-glutamyl-, monomer, CS-0655365, Q27140594, (4S)-4-amino-5-[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]-5-oxopentanoic acid, Melanin synthesized from Glu-Tyr substrate catalyzed by tyrosinase for 40 hrs, (4S)-4-amino-5-[[(1S)-2-hydroxy-1-[(4-hydroxyphenyl)methyl]-2-oxo-ethyl]amino]-5-oxo-pentanoic acid, E-Y |
|---|---|
| Topological Polar Surface Area | 150.0 |
| Hydrogen Bond Donor Count | 5.0 |
| Inchi Key | YSWHPLCDIMUKFE-QWRGUYRKSA-N |
| Rotatable Bond Count | 8.0 |
| State | Solid |
| Synonyms | alpha-Glu-tyr, alpha-Glutamyltyrosine, alpha-L-Glu-L-tyr, E-Y, EY, L-Glu-L-tyr, a-Glu-tyr, Α-glu-tyr, a-Glutamyltyrosine, Α-glutamyltyrosine, a-L-Glu-L-tyr, Α-L-glu-L-tyr, Α-L-glutamyl-L-tyrosine, L-Α-glutamyl-L-tyrosine, N-Α-glutamyltyrosine, N-Α-L-glutamyl-L-tyrosine, N-L-Α-glutamyltyrosine, N-L-Α-glutamyl-L-tyrosine, alpha-L-Glutamyl-L-tyrosine, L-alpha-Glutamyl-L-tyrosine, N-alpha-Glutamyltyrosine, N-alpha-L-Glutamyl-L-tyrosine, N-L-alpha-Glutamyltyrosine, N-L-alpha-Glutamyl-L-tyrosine, NSC 523821, Glu-tyr, L-Glutamyl-L-tyrosine, N-Glutamyltyrosine, N-L-Glutamyl-L-tyrosine, Glutamyl-tyrosine, Glutamic acid tyrosine dipeptide, Glutamate tyrosine dipeptide, Glutamic acid-tyrosine dipeptide, Glutamate-tyrosine dipeptide, e-Y dipeptide, EY dipeptide, Glutamyltyrosine |
| Heavy Atom Count | 22.0 |
| Compound Name | H-Glu-Tyr-OH |
| Kingdom | Organic compounds |
| Description | Glutamyltyrosine, also known as alpha-glu-tyr or E-Y, is a member of the class of compounds known as dipeptides. Dipeptides are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Glutamyltyrosine is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Glutamyltyrosine can be found in soy bean, which makes glutamyltyrosine a potential biomarker for the consumption of this food product. Glutamyltyrosine can be found primarily in feces. |
| Exact Mass | 310.116 |
| Formal Charge | 0.0 |
| Monoisotopic Mass | 310.116 |
| Isotope Atom Count | 0.0 |
| Molecular Complexity | 406.0 |
| Hydrogen Bond Acceptor Count | 7.0 |
| Molecular Weight | 310.3 |
| Database Name | fooddb_chem_all;hmdb_chem_all;pubchem |
| Covalent Unit Count | 1.0 |
| Defined Atom Stereocenter Count | 2.0 |
| Iupac Name | (4S)-4-amino-5-[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]-5-oxopentanoic acid |
| Total Atom Stereocenter Count | 2.0 |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Total Bond Stereocenter Count | 0.0 |
| Class | Carboxylic acids and derivatives |
| Inchi | InChI=1S/C14H18N2O6/c15-10(5-6-12(18)19)13(20)16-11(14(21)22)7-8-1-3-9(17)4-2-8/h1-4,10-11,17H,5-7,15H2,(H,16,20)(H,18,19)(H,21,22)/t10-,11-/m0/s1 |
| Smiles | C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)N)O |
| Xlogp | -3.8 |
| Superclass | Organic acids and derivatives |
| Defined Bond Stereocenter Count | 0.0 |
| Subclass | Amino acids, peptides, and analogues |
| Taxonomy Direct Parent | Dipeptides |
| Molecular Formula | C14H18N2O6 |
- 1. Outgoing r'ship
FOUND_INto/from Glycine Max (Plant) Rel Props:Source_db:fooddb_chem_all